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Regulatory Requirement LOGIQ e complies with regulatory requirements of the following European Directive 93/42/EEC concerning medical devices. Manufacturer GE Medical Systems (China) Co., Ltd. No. 19 Changjiang Road Wuxi National Hi-Tech Development Zone Jiangsu, P.R.China 214028 Tel: +86 510 85225888; Fax: +86 510 85226688 GE Healthcare GE Medical System: Telex 3797371 P. O. Box 414, Milwaukee, Wisconsin 53201 U.S.A. (Asia, Pacific, Latin America, North America) GE Ultraschall:Tel: +33 (0) 130 831 300 Deutschland GmbH & Co KG Beethovenstrabe 239, Postfach 11 05 60 D-42655 Solingen, Germany